Canonical Allele Identifier: CA396471008

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68863614A>G (hg19) ; chr16:g.68829711A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829711A>G , CM000678.2:g.68829711A>G	GRCh38
NC_000016.9:g.68863614A>G , CM000678.1:g.68863614A>G	GRCh37
NC_000016.8:g.67421115A>G	NCBI36
NG_008021.1:g.97420A>G , LRG_301:g.97420A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2353A>G MANE Select	ENSP00000261769.4:p.Asn785Asp
ENST00000261769.9:c.2353A>G	ENSP00000261769.4:p.Asn785Asp
ENST00000422392.6:c.2170A>G	ENSP00000414946.2:p.Asn724Asp
ENST00000562118.1:n.571A>G
ENST00000562836.5:n.2424A>G
ENST00000566510.5:c.*1019A>G	ENSP00000458139.1:n.*1019A>G
ENST00000566612.5:c.*593A>G	ENSP00000454782.1:n.*593A>G
ENST00000611625.4:c.2416A>G	ENSP00000481063.1:p.Asn806Asp
ENST00000612417.4:c.1853+3157A>G	ENSP00000478360.1:n.1853+3157A>G
ENST00000621016.4:c.1866-4492A>G	ENSP00000480664.1:n.1866-4492A>G
NM_004360.3:c.2353A>G , LRG_301t1:c.2353A>G	NP_004351.1:p.Asn785Asp
XM_011523488.1:c.1618A>G	XP_011521790.1:p.Asn540Asp
XM_011523489.1:c.1618A>G	XP_011521791.1:p.Asn540Asp
NM_001317184.1:c.2170A>G	NP_001304113.1:p.Asn724Asp
NM_001317185.1:c.805A>G	NP_001304114.1:p.Asn269Asp
NM_001317186.1:c.388A>G	NP_001304115.1:p.Asn130Asp
NM_004360.4:c.2353A>G	NP_004351.1:p.Asn785Asp
NM_004360.5:c.2353A>G MANE Select	NP_004351.1:p.Asn785Asp
NM_001317184.2:c.2170A>G	NP_001304113.1:p.Asn724Asp
NM_001317185.2:c.805A>G	NP_001304114.1:p.Asn269Asp
NM_001317186.2:c.388A>G	NP_001304115.1:p.Asn130Asp